856120-87-1 Usage
Description
(6-azidohex-1-yn-1-yl)benzene, with the molecular formula C13H13N3, is a chemical compound belonging to the alkyne functional group. It features a benzene ring connected to a six-carbon alkyne chain, with an azide group at the terminal end. (6-azidohex-1-yn-1-yl)benzene is known for its versatility in organic synthesis and its potential applications in various scientific fields.
Uses
Used in Organic Synthesis:
(6-azidohex-1-yn-1-yl)benzene is used as a building block in the preparation of various azide-alkyne click chemistry reactions. Its azide group enables a range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (6-azidohex-1-yl)benzene is used as a key intermediate for the development of new drugs. Its unique structure and reactivity contribute to the design and synthesis of potential therapeutic agents.
Used in Materials Science:
(6-azidohex-1-yn-1-yl)benzene is employed as a component in the development of novel materials with specific properties. Its incorporation into material systems can lead to advancements in areas such as polymer science and nanotechnology.
Used in Bioconjugation Chemistry:
In the field of bioconjugation chemistry, (6-azidohex-1-yn-1-yl)benzene is used as a linker or modifier to attach biologically relevant molecules, such as proteins or nucleic acids, to other chemical entities. This allows for the creation of bioconjugates with tailored properties and functions.
Used in Chemical Biology and Medicinal Chemistry Research:
The unique structure and reactivity of (6-azidohex-1-yn-1-yl)benzene make it a valuable compound for research and development in chemical biology and medicinal chemistry. It can be utilized in the study of biological processes and the design of new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 856120-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,1,2 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 856120-87:
(8*8)+(7*5)+(6*6)+(5*1)+(4*2)+(3*0)+(2*8)+(1*7)=171
171 % 10 = 1
So 856120-87-1 is a valid CAS Registry Number.
856120-87-1Relevant articles and documents
A Commercially Available and User-Friendly Catalyst for Hydroamination Reactions under Technical Conditions
Zelenay, Benjamin,Munton, Peter,Tian, Xiaojie,Díez-González, Silvia
supporting information, p. 4725 - 4730 (2019/08/01)
The activity of a simple, commercially available copper salt, [Cu(NCMe)4](BF4) in intramolecular hydroamination reactions of alkynes and allenes is presented. Reactions were successfully carried out in technical acetonitrile in the presence of air. While attempts of alkene hydroamination failed, this catalyst was also found active in intermolecular aza-Michael reactions.
The acid-mediated intramolecular 1,3-dipolar cycloaddition of derived 2-nitro-1,1-ethenediamines for the synthesis of novel fused bicyclic isoxazoles
Page, Lee W.,Bailey, Matthew,Beswick, Paul J.,Frydrych, Simon,Gleave, Robert J.
scheme or table, p. 3388 - 3391 (2010/09/05)
The discovery of a novel synthesis of new fused bicyclic isoxazoles, for example, N-methyl-3-phenyl-5,6-dihydro-4H-isoxazolo[3,4-c]azepin-8-amine (2a), N-methyl-3-phenyl-4,5-dihydroisoxazolo[3,4-c]pyridin-7-amine (2b) and N-methyl-3-phenyl-4H-pyrrolo[3,4-
Intramolecular hydroamination of alkynes catalyzed by Pd(PPh 3)4/triphenylphosphine under neutral conditions
Bajracharya, Gan B.,Huo, Zhibao,Yamamoto, Yoshinori
, p. 4883 - 4886 (2007/10/03)
The intramolecular hydroamination of alkynes tethered with amino group 1 in the presence of catalytic amounts of Pd(PPh3)4 and PPh3 in benzene at 100°C proceeded smoothly without the use of any additional acid source to af
